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激光激活的金纳米壳体外消融前列腺癌细胞的疗效。

Efficacy of laser-activated gold nanoshells in ablating prostate cancer cells in vitro.

作者信息

Stern Joshua M, Stanfield Jennifer, Lotan Yair, Park Sangtae, Hsieh Jer-Tsong, Cadeddu Jeffrey A

机构信息

Department of Urology, The University of Texas, Southwestern Medical Center, Dallas Texas, 75390-9110, USA.

出版信息

J Endourol. 2007 Aug;21(8):939-43. doi: 10.1089/end.2007.0437.

Abstract

BACKGROUND AND PURPOSE

Nanoshells (NS) are nanoparticles consisting of a dielectric silica core covered by a thin gold shell. Nanoshells can be designed to absorb near-infrared (NIR) light strongly to generate heat and provide optically guided hyperthermic ablation. Laser-activated gold nanoshells (LAGN) may offer a minimally invasive targeted ablative treatment for prostate cancer. We studied the in-vitro effectiveness of LAGN ablation on human prostate cancer cells.

MATERIALS AND METHODS

Two human prostate cancer (PCa) cell lines, PC-3 and C4-2, were grown to 80% confluency in T medium with 5% fetal bovine serum. In order to determine a threshold concentration of gold nanoshells (GNS) needed to achieve full cellular ablation, dose titration was performed. In subsequent experiments, GNS were added to PCa cells in phosphate-buffered saline at concentrations above the predetermined threshold. The cells were then exposed to NIR light (810 nm, 88 W/cm2) for 5 minutes and stained immediately for viability using the Calcein AM assay. For determining long-term cell survival, the crystal violet assay was employed.

RESULTS

The GNS could be evenly distributed across the culture plates. A ratio of 5000 GNS per PCa cell was critical for achieving cell kill. Cells treated with GNS + NIR demonstrated a laser-specific zone of cell death. The crystal violet viability assay confirmed consistent cell death rather than induction of cell dormancy. Cells treated with GNS alone or with NIR light alone demonstrated no toxicity.

CONCLUSION

Laser-activated gold nanoshells can ablate human PCa cells in vitro. This nanoparticle technology is an attractive therapeutic agent for selective tumor ablation.

摘要

背景与目的

纳米壳(NS)是由介电二氧化硅核心和薄金壳组成的纳米颗粒。纳米壳可被设计为强烈吸收近红外(NIR)光以产生热量,并提供光引导的热消融。激光激活金纳米壳(LAGN)可能为前列腺癌提供一种微创靶向消融治疗。我们研究了LAGN消融对人前列腺癌细胞的体外有效性。

材料与方法

两种人前列腺癌(PCa)细胞系PC-3和C4-2在含5%胎牛血清的T培养基中培养至80%汇合。为了确定实现完全细胞消融所需的金纳米壳(GNS)阈值浓度,进行了剂量滴定。在后续实验中,将GNS以高于预定阈值的浓度添加到磷酸盐缓冲盐水中的PCa细胞中。然后将细胞暴露于近红外光(810 nm,88 W/cm2)下5分钟,并立即使用钙黄绿素AM测定法染色以检测细胞活力。为了确定细胞的长期存活情况,采用了结晶紫测定法。

结果

GNS可均匀分布在培养板上。每个PCa细胞5000个GNS的比例对于实现细胞杀伤至关重要。用GNS + NIR处理的细胞表现出激光特异性的细胞死亡区域。结晶紫活力测定证实了持续的细胞死亡而非细胞休眠的诱导。单独用GNS或单独用近红外光处理的细胞均未显示出毒性。

结论

激光激活金纳米壳可在体外消融人PCa细胞。这种纳米颗粒技术是一种有吸引力的选择性肿瘤消融治疗剂。

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